Data / Medical devices / Bur, Dental / Switzerland
FDA-registered makers of Bur, Dental in Switzerland: 12 establishments
12 establishments in Switzerland are registered with the FDA to make Bur, Dental (product code EJL). 0 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 2, 2026.
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- Device
- Bur, Dental
- Product code
- EJL
- Country
- Switzerland
Makers of Bur, Dental in Switzerland
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| CAMLOG Biotechnologies GmbH | Basel Basel-Stadt, Switzerland | Exporter to the US, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Cendres+metaux SA | Biel/Bienne Bern, Switzerland | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Coltene/Whaledent AG | ALTSTAETTEN Sankt Gallen, Switzerland | Manufacturer | 0 | 0 | 1 | 0 | api.fda.gov | |
| CeramTec Schweiz GmbH | Spreitenbach Aargau, Switzerland | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Dent4you AG | Heerbrugg Sankt Gallen, Switzerland | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Diaswiss S.A. | NYON Vaud, Switzerland | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Institut Straumann AG | BASEL Basel-Stadt, Switzerland | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Jota AG | RUETHI, SG Sankt Gallen, Switzerland | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Maillefer Instruments Holding Sarl | BALLAIGUES Vaud, Switzerland | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| SDS Swiss Dental Solutions | Kreuzlingen Thurgau, Switzerland | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sphinx Tools Ltd | Derendingen Solothurn, Switzerland | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Straumann Villeret SA | VILLERET Bern, Switzerland | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.